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Characterization of two mutations in the SPTLC1 subunit of serine palmitoyltransferase associated with hereditary sensory and autonomic neuropathy type I

✍ Scribed by Annelies Rotthier; Anke Penno; Bernd Rautenstrauss; Michaela Auer-Grumbach; Georg M. Stettner; Bob Asselbergh; Kim Van Hoof; Heinrich Sticht; Nicolas Lévy; Vincent Timmerman; Thorsten Hornemann; Katrien Janssens


Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
615 KB
Volume
32
Category
Article
ISSN
1059-7794

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